rs193303002

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs193303002(A;A)

Make rs193303002(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15927

is a	snp
is	mentioned by
dbSNP	rs193303002
dbSNP (classic)	rs193303002
ClinGen	rs193303002
ebi	rs193303002
HLI	rs193303002
Exac	rs193303002
Gnomad	rs193303002
Varsome	rs193303002
LitVar	rs193303002
Map	rs193303002
PheGenI	rs193303002
Biobank	rs193303002
1000 genomes	rs193303002
hgdp	rs193303002
ensembl	rs193303002
geneview	rs193303002
scholar	rs193303002
google	rs193303002
pharmgkb	rs193303002
gwascentral	rs193303002
openSNP	rs193303002
23andMe	rs193303002
SNPshot	rs193303002
SNPdbe	rs193303002
MSV3d	rs193303002
GWAS Ctlg	rs193303002

Merged from

Rs527236197

Max Magnitude

0

ClinVar
Risk	rs193303002(A;A)
Alt	rs193303002(A;A)
Reference	Rs193303002(G;G)
Significance	Probable-Pathogenic
Disease	Familial cancer of breast
Variation	info
Gene
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_012920.1:m.15927G>A
CLNSRC
CLNACC	RCV000133441.1,